| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| von Willebrand disease, type IIH |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| hémoglobinose E (trouble) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| X chromosome-linked pyridoxine responsive sideroblastic anemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired coagulation factor deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Mild hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Failed attempted termination of pregnancy with afibrinogenaemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| High molecular weight kininogen deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Immune thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Thrombocytopenia due to extracorporeal circulation (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Legal termination of pregnancy with afibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Severe combined immunodeficiency disease |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
| Hereditary factor I deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Illegal termination of pregnancy with afibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Transient neonatal disorder of coagulation |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Factor XI deficiency, type II |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Post infectious thrombocytopenic purpura |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor II deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Moderate hereditary factor VIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired factor X deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
| Thrombocytopenia caused by hypothermia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Disseminated intravascular coagulation in newborn |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Failed attempted termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| von Willebrand disease, type IID |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Abortion with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired factor XI deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired factor V deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Antithrombin III deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Severe combined immunodeficiency due to absent adenosine deaminase (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
| Factor VII deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor X deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Sex-linked thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Familial multiple factor deficiency syndrome, type V |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Proaccelerin deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Labile factor deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Placement of choledochal stent |
Procedure site - Indirect (attribute) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
| Factor XI inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| anémie hémolytique héréditaire |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor VII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| von Willebrand factor inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| HNSHA due to phosphofructokinase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired hypoprothrombinemia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Factor V inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor IX deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Secondary cryofibrinogenaemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Factor V deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor XII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| surdosage en anticoagulant |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Adenosine deaminase deficiency |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
| Hereditary dysfibrinogenemia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Severe combined immunodeficiency due to absent interleukin-2 production (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
| Factor XI deficiency, type III |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Haemoglobin E trait |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Factor XII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| trouble d'inhibition du facteur VIII |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Warfarin overdosage (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Cyclic thrombocytopenia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Prekallikrein deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Postpartum coagulation defect with haemorrhage |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Severe combined immunodeficiency due to absent T cell receptor (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
1 |
| Hereditary factor XI deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Thrombocytopenia due to blood loss (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary factor XIII deficiency disease (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| hémoglobinose C (trouble) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Dilutional thrombocytopenia (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| von Willebrand disease, type IIE (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Nezelof's syndrome (disorder) |
localisation d'une constatation (attribut) |
True |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
| Factor I inhibitor disorder (disorder) |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired pancytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| HNSHA due to phosphoglycerate kinase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary elliptocytosis due to deficiency of protein 4.1 |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Abscess of external nose |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
2 |
| Mediterranean macrothrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Familial multiple factor deficiency syndrome, type VI |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Thalassemia-hemoglobin C disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Primary cryofibrinogenemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Illegal termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| HNSHA due to diphosphoglycerate mutase deficiency |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary sideroblastic anemia |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Defibrination syndrome following molar AND/OR ectopic pregnancy |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Thrombocytopenia due to hypersplenism |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired factor XIII deficiency disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Familial multiple factor deficiency syndrome, type III |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Acquired coagulation factor inhibitor disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Blood coagulation disorder |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Familial multiple factor deficiency syndrome, type II |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hereditary elliptocytosis due to beta spectrin-ankyrin interaction |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Thrombocytosis |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Legal termination of pregnancy with defibrination syndrome |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Hemoglobin D disease |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|
| Familial multiple factor deficiency syndrome, type IV |
localisation d'une constatation (attribut) |
False |
structure d'un système corporel |
Inferred relationship |
Some |
|